SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

Similar documents
SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

100 ml of the syrup contain 825 mg of ivy leaf dry extract (Hedera helix L., folium) ( 4-8:1). Extraction solvent: ethanol 30% (m/m).

Summary of Product Characteristics Updated 01-May-2015 Meda Pharmaceuticals

SUMMARY OF PRODUCT CHARACTERISTICS 2. QUALITATIVE AND QUANTITATIVE COMPOSITION

Used for removing granulation tissue, warts (including verrucas), for cautery and as a caustic

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

1. NAME OF THE MEDICINAL PRODUCT. Lamisil 1% cutaneous solution. 2. QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

Summary of Product Characteristics

1. NAME OF THE MEDICINAL PRODUCT. Vicks Sinex, 0.5 mg/ml, nasal spray solution 2. QUALITATIVE AND QUANTITATIVE COMPOSITION

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

Summary of Product Characteristics

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS

3 PHARMACEUTICAL FORM Coated tablet Round, white to off-white, sugar coated tablets, plain on both sides.

NEW ZEALAND DATA SHEET

SUMMARY OF PRODUCT CHARACTERISTICS 2. QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS

For a full list of excipients, see section 6.1. A sterile, clear, bright, colourless, aqueous solution.

Instil one or two drops in the conjunctival sac(s) every three to four hours as needed.

Summary of Product Characteristics

SUMMARY OF PRODUCT CHARACTERISTICS

Summary of Product Characteristics

2. QUALITATIVE AND QUANTITATIVE COMPOSITION

Summary of Product Characteristics

Body weight more than 30kg : 10ml (10mg) of the syrup once daily.

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS. 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each sachet contains the following active ingredients:

SUMMARY OF THE PRODUCT CHARACTERISTICS. The content of electrolyte ions per sachet when made up to 125 ml of solution.

SUMMARY OF PRODUCT CHARACTERISTICS

VALERIANA OFFICINALIS 445 MG COATED TABLET Summary of Product Characteristics

Summary of Product Characteristics

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS

Excipients with known effect: Each gramme of gel contains 1 mg methyl parahydroxybenzoate (E-218) and 0.5 mg propyl parahydroxybenzoate (E-216).

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

Summary of Product Characteristics

SUMMARY OF PRODUCT CHARACTERISTICS 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

NAPHCON-A Eye Drops naphazoline hydrochloride 0.025% and pheniramine maleate 0.3%.

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS

Health Products Regulatory Authority

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

Summary of Product Characteristics

Summary of Product Characteristics

SUMMARY OF THE PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS 2. QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT

PDF rendering: Titel , Version 1.1, Namn Azelastine OmniVision 0.5 mg per ml eye drops, solution SmPC

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS. A 2.5ml single-dose bottle containing IU Cholecalciferol (equivalent to 625 micrograms vitamin D 3 )

NEW ZEALAND DATA SHEET

2. QUALITATIVE AND QUANTITATIVE COMPOSITION. Each capsule contains PARACETAMOL 500mg For a full list of excipients, see section 6.1.

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

NEW ZEALAND DATA SHEET 1. PRODUCT NAME

SUMMARY OF PRODUCT CHARACTERISTICS

2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each sachet of Macrovic Junior powder for oral solution contains the following active ingredients:

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2. QUALITATIVE AND QUANTITATIVE COMPOSITION

NEW ZEALAND DATA SHEET

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

Health Products Regulatory Authority

SUMMARY OF PRODUCT CHARACTERISTICS. Albuman 40 g/l is a solution containing 40 g/l (4%) of total protein of which at least 95% is human albumin.

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

For the use only of a Registered Medical Practitioner or a Hospital or a Laboratory. Light Liquid Paraffin and White Soft Paraffin Cream

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS

ADT Booster Data Sheet

SUMMARY OF PRODUCT CHARACTERISTICS

Indications: For the treatment and control of fascioliasis in cattle and sheep.

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS. Synthamin 14, 8.5% Amino Acid Intravenous Infusion

European Medicines Agency. Superseded COMMITTEE ON HERBAL MEDICINAL PRODUCTS (HMPC) FINAL COMMUNITY HERBAL MONOGRAPH ON SALVIA OFFICINALIS L.

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS

SUMMARY OF PRODUCT CHARACTERISTICS. for. Felden, gel

2. QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS

Produktinformationen för Bentifen, 0,25 mg/ml, Ögondroppar, lösning, endosbehållare, MTnr 16252, gäller vid det tillfälle då läkemedlet godkändes.

Transcription:

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Peroxyl Mouthwash. 2 QUALITATIVE AND QUANTITATIVE COMPOSITION 100ml of solution contains 1.5g of Hydrogen peroxide (as 30% Hydrogen Peroxide solution). For a full list of excipients, see section 6.1 3. PHARMACEUTICAL FORM Mouthwash A clear aqua-blue liquid 4. CLINICAL PARTICULARS 4.1. Therapeutic Indications As a cleanser in the symptomatic relief of minor mouth and gum irritations. 4.2 Posology and method of administration Do not use in children under the age of 6. Peroxyl is ready to use. Rinse with 10 ml (one capful, 10 ml line within cap) for approximately one minute, then spit out. Use 3 times daily (after meals and at bedtime) or as directed by a doctor or dentist. Adults and children over 12 years: as above. Children between 6-12 years old: Use under the supervision of an adult. The duration of the treatment should not exceed 7 days. Method of administration: Oromucosal use.

4.3. Contraindications This medicinal product must not be used in cases of hypersensitivity of the active substance or to any of the excipients. 4.4. Special warning and precautions for use DO NOT SWALLOW. If irritation persists for 7 days, is severe, is due to orthodontic appliances and/or dentures, or swelling or fever develops, the patient's condition needs to be re-evaluated by a doctor or dentist. Overdose can injure the gums and continued use of hydrogen peroxide may cause reversible hypertrophy of the papillae of the tongue known as black hairy tongue therefore using this product at high doses or for long periods of time is not recommended. Avoid contact with eyes. 4.5 Interaction with other medicinal products and other forms of interaction None known 4.6. Pregnancy and Lactation Although there are not sufficient specific clinical data on the use of Peroxyl in this patient group, self-administration without medical advice is not recommended. 4.7. Effects on ability to drive and use machines Not relevant 4.8 Undesirable effects

Some cases of mucosal irritation and swelling of the oral tissues have been reported specially with high doses or in continued use (see special warnings, above). The symptoms will resolve on stopping treatment with Peroxyl. Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via Yellow Card Scheme at: www.mhra.gov.uk/yellowcard. 4.9. Overdose Peroxyl is a dilute hydrogen peroxide solution and is unlikely to cause the symptoms of overdosage associated with strong solutions (30-40%). Peroxyl contains levo-menthol which if accidentally ingested at excessive amounts may cause convulsions, particularly in infants and children. 5. PHARMACOLOGICAL PROPERTIES 5.1. Pharmacodynamic properties Pharmacotherapeutic group: Antiinfectives and antiseptics for local oral treatment ATC code: A01AB02 Hydrogen peroxide is an oral antiseptic cleanser. The principal action is brought about by contact of hydrogen peroxide with peroxidases and catalases present in tissues and saliva, which causes the rapid release of oxygen. This provides mechanical cleansing which flushes out mouth debris, and helps in the treatment of oral irritations. 5.2. Pharmacokinetic Properties In the mouth, salivary peroxidase breaks down hydrogen peroxide to release water and oxygen. 5.3. Pre-clinical Safety Data Low doses of hydrogen peroxide do not produce tissue damage or result in neoplastic changes. Application of Peroxyl to abraded mucosa in the hamster cheek pouch study over 21 days showed no adverse effect.

Hydrogen peroxide is not genotoxic in animals. The available data on reproductive toxicology are incomplete but do not indicate an effect at low concentrations. 6. PHARMACEUTICAL PARTICULARS 6.1. List of excipients Purified Water Sorbitol 70%w/w (non-crystallising) Ethanol 96% Poloxamer 388 Polysorbate 20 Methyl salicylate Levo-Menthol Sodium saccharin Brilliant Blue FCF (E133) 6.2. Incompatibilities Not applicable. 6.3 Shelf life 24 months (300 ml pack size) 6.4. Special Precautions for Storage Do not store above 25 C. 6.5 Nature and contents of container 300 ml in bottle (PET), with polyethylene cap 6.6. Special precautions for disposal No special requirements

7. MARKETING AUTHORISATION HOLDER Colgate-Palmolive (UK) Ltd Guildford Business Park Middleton Road Guildford Surrey GU2 8JZ UK 8. MARKETING AUTHORISATION NUMBER(S) PL 00049/0038 9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION 29/11/2006 10 DATE OF REVISION OF THE TEXT 17/02/2016